Structural simplification: an efficient strategy in lead optimization

被引:3
|
作者
Shengzheng Wang [1 ,2 ]
Guoqiang Dong [1 ]
Chunquan Sheng [1 ]
机构
[1] Department of Medicinal Chemistry, School of Pharmacy, Second Military Medical University
[2] Department of Medicinal Chemistry and Pharmaceutical Analysis, School of Pharmacy, Fourth Military Medical University
基金
中国国家自然科学基金;
关键词
Structural simplification; Lead optimization; Drug discovery; Drug design; Reducing rings number; Reducing chiral centers; Structure-based simplification; Pharmacophore-based simplification;
D O I
暂无
中图分类号
R91 [药物基础科学];
学科分类号
1007 ;
摘要
The trend toward designing large hydrophobic molecules for lead optimization is often associated with poor drug-likeness and high attrition rates in drug discovery and development. Structural simplification is a powerful strategy for improving the efficiency and success rate of drug design by avoiding "molecular obesity". The structural simplification of large or complex lead compounds by truncating unnecessary groups can not only improve their synthetic accessibility but also improve their pharmacokinetic profiles, reduce side effects and so on. This review will summarize the application of structural simplification in lead optimization. Numerous case studies, particularly those involving successful examples leading to marketed drugs or drug-like candidates, will be introduced and analyzed to illustrate the design strategies and guidelines for structural simplification.
引用
收藏
页码:880 / 901
页数:22
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